Method for Producing Virus-Type Particles Containing an Active Substance

• US 20090215146A1
• Filed: 03/28/2006
• Published: 08/27/2009
• Est. Priority Date: 05/24/2005
• Status: Abandoned Application

• Current Assignee: Responsif GmbH
• Original Assignee: Responsif GmbH
• Inventors: Reiser, Cristian, Rühland, Claus, Reichel, Christoph, Hess, Jurgen
• Application Number:
  US11/915,475
• Publication Number:
  US 20090215146A1
• Time in Patent Office: Days
• US Class Current: 435/235.100
• CPC Class Codes: A61K 2039/5256 expressing foreign proteins
• CPC Class Codes: C07K 14/005 from viruses
• CPC Class Codes: C07K 2319/00 Fusion polypeptide
• CPC Class Codes: C12N 2710/22022 New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
• CPC Class Codes: C12N 2710/22023 Virus like particles [VLP]
• CPC Class Codes: C12N 2710/22051 Methods of production or purification of viral material
• CPC Class Codes: C12N 7/00 Viruses; Bacteriophages; Compositions thereof; Preparation or purification thereof preparing medicinal viral antigen or antibody compositions, e.g. virus vaccines, A61K39/00
• CPC Class Codes: Y02A 50/30 Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Abstract

The invention relates to a method for producing virus-type particles containing an active substance. Proteins, which comprise a first amino acid sequence which is derived from a first virus protein, and fusion proteins are assembled in order to form the virus-type particles. The proteins and the fusion proteins are coexpressed in yeast cells.

Claims

1. A method for producing virus-type particles containing an active substance, proteins each having a first amino acid sequence which is derived from a first virus protein and fusion proteins assemble to the virus-type particles, the first amino acid sequence being an amino acid sequence which is adequate for the formation of capsoid-forming capsomers that specifically bind a second virus protein, the fusion proteins having a second amino acid sequence each derived from the second virus protein and specifically binding to one of the capsomers each and a third amino acid sequence which forms the active substance, the proteins and the fusion proteins being co-expressed in yeast cells.

2. A method according to claim 1, wherein the first virus protein and/or the second virus protein stems/stem from a virus or can be obtained from the same, the virus being selected from the group of the non-enveloped viruses, comprising Papovaviridae, in particular Polyoma and Papilloma viruses, Iridoviridae, Adenoviridae, Parvoviridae, Picornaviridae, in particular polio viruses, Caliciviridae, Reoviridae and Birnaviridae.

3. A method according to any of the preceding claims, the first virus protein being the virus protein 1 of the polyoma virus (VP1) and the second virus protein being the virus protein 2 (VP2) or the virus protein 3 (VP3) of the polyoma virus.

4. A method according to any of the preceding claims, the capsomers having the form of pentamers, hexamers or heptamers.

5. A method according to any of the preceding claims, the third amino acid sequence being, at least predominantly, hydrophobic.

6. A method according to any of the preceding claims, the third amino acid sequence forming the N terminal end of the fusion protein.

7. A method according to any of the preceding claims, wherein in the course of the co-expression of the proteins and of the fusion proteins the respective extent of the expression of the proteins and of the fusion proteins is harmonised in such a way that in the course of the method the biggest possible amount of the virus-type particles containing the active substance is formed.

8. A method according to claim 7, the expression of the proteins taking place under the control of a first promotor contained in a first plasmid, which is coding for the proteins and the expression of the fusion proteins taking place under the control of a second promotor contained in a plasmid, which is coding for the fusion proteins, the respective extent of the expression of the proteins and of the fusion proteins being harmonised by means of a suitable selection of the first and of the second promotor.

9. A method according to claim 8, the first and/or the second promotor being selected from a group consisting of the promotors of the genes of alcohol dehydrogenase 1 (ADH1), alcohol dehydrogenase 2 (ADH2), orthophosphoric monoester phosphohydrolase (Apase), format dehydrogenase (FOD), galactokinase (GAL1), UDP glucose-4-epimerase (GAL10), glyceraldehyd-3-phosphate (GAP), glyceraldehyd-phosphate dehydrogenase (GAPDH), alcohol oxidase (AOX), methanol oxidase (MOX), no message in thiamine 1 (NMT1), 3-phosphoglycerate-kinase (PGK) and pyruvatekinase (PYK1) as well as the hybrid promotors GAL10/PYK1 and ADH2/GAPDH.

10. A method according to any of the preceding claims, the third amino acid sequence comprising a sequence of at least one antigen, in particular a tumor-associated antigen, of at least one epitope of this antigen or of different epitopes of the said antigen.

11. A method according to claim 10, the tumor-associated antigen being selected from the group comprising NY-ESO-I, Telomerase Reverse Transcriptase (TERT), p53, MDM2, CYP1B1, HER-2/new, CEACAM (carcinoembryonic antigen-related cell adhesion molecule 5) and the apoptosis inhibiting protein Survivin.

12. A method according to any of the claims 1 to 10, the antigen being an antigen of a pathogen of a virus disease, in particular, a chronic one, or of an infectious disease.

13. A method according to claim 12, the antigen being selected from a group comprising HIV-associated antigen, HCV-associated antigen, tuberculosis-associated antigen, in particular Ag85A, Ag85B, Rv3407, Esat-6 and Hsp65, malaria-associated antigen, in particular CSP-1, LSA-1, LSA-3 and EXP-1, an antigen associated with a merozoite stage of the malarial parasite, in particular MSP-1, and bilharziosis-associated antigen.

14. A method according to any of the preceding claims, the third amino acid sequence forming an MHC-Class I-specific antigen.

15. A method according to any of the claims 3 to 14, wherein the first amino acid sequence which is derived from the virus protein 1 of the polyoma virus (VP1) does not have the DNA-binding domain contained in the VP1 and/or does not have the nuclear localisation sequence (NLS) contained in the VP1.

16. A method according to any of the preceding claims, the yeast cells being yeast cells of the species Saccharomyces cerevisiae, Schizosaccharomyces pombe, Pichia pastoris, Hansenula polymorpha, Kluyveromyces lactis or Kluyveromyces marxianus.

17. Virus-type particles containing proteins each having a first amino acid sequence which is derived from a first virus protein, and fusion proteins, the first amino acid sequence being an amino acid sequence which is adequate for the formation of capsoid-forming capsomers which specifically bind a second virus protein, the fusion proteins having a second amino acid sequence each which is derived from the second virus protein and specifically binds to one of the capsomers each and a predominantly hydrophobic third amino acid sequence which forms an active substance.

18. Particles according to claim 17, wherein the first virus protein and/or the second virus protein stems/stem from a virus or can be obtained from the same, that is selected from the group of the non-enveloped viruses, comprising Papovaviridae, in particular Polyoma and Papilloma viruses, Iridoviridae, Adenoviridae, Parvoviridae, Picornaviridae, in particular polio viruses, Caliciviridae, Reoviridae and Birnaviridae.

19. Particles according to any of the claims 17 or 18, the first virus protein being the virus protein 1 of the polyoma virus (VP1) and the second virus protein being the virus protein 2 (VP2) or the virus protein 3 (VP3) of the polyoma virus.

20. Particles according to any of the claims 17 to 19, the capsomers having the form of pentamers, hexamers or heptamers.

21. Particles according to any of the claims 17 to 20, the third amino acid sequence forming the N terminal end of the fusion protein.

22. Particles according to any of the claims 17 to 21, the third amino acid sequence comprising a sequence of at least one antigen, in particular a tumor-associated antigen, of at least one epitope of this antigen or of different epitopes of the said antigen.

23. Particles according to claim 22, the tumor-associated antigen being selected from the group comprising NY-ESO-I, Telomerase Reverse Transcriptase (TERT), p53, MDM2, CYP1B1, HER-2/new, CEACAM (carcinoembryonic antigen-related cell adhesion molecule 5) and the apoptosis inhibiting protein Survivin.

24. Particles according to any of the claims 17 to 22, the antigen being an antigen of a pathogen of a virus disease, in particular, a chronic one, or of an infectious disease.

25. Particles according to claim 24, the antigen being selected from a group comprising HIV-associated antigen, HCV-associated antigen, tuberculosis-associated antigen, in particular Ag85A, Ag85B, Rv3407, Esat-6 and Hsp65, malaria-associated antigen, in particular CSP-1, LSA-1, LSA-3 and EXP-1, an antigen associated with a merozoite stage of the malarial parasite, in particular MSP-1, and bilharziosis-associated antigen.

26. Particles according to any of the claims 17 to 25, the third amino acid sequence forming an MHC-Class I-specific antigen.

27. Particles according to any of the claims 19 to 26, where the first amino acid sequence which is derived from the virus protein 1 of the polyoma virus does not have the DNA-binding domain contained in the virus protein 1 and/or does not have the nuclear localisation sequence (NLS) contained in the virus protein 1.

28. Particles according to any of the claims 17 to 27 for use as a medicament.